تفاعل #314384
ord-fdb1c49ab6034e68adfb0fa4e76d350e
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المعالجة
- 1workup.WAITfollowed by 4 hours
- 2workup.STIRRINGof stirring
- 3أخرىThe obtained particles (precursor of Example 1-2) are purified in water by means of dialysis
- 4workup.ADDITIONThese particles are then dispersed in tetrahydrofuran (30 ml)/dimethylformamide (10 ml)
- 5workup.ADDITIONa tetrahydrofuran (10 ml)/dimethylformamide (50 ml) solution of dicyclohexylcarbodiimide (800 mg), hydroxybenzotriazole (500 mg), and 2,2′-(ethylenedioxy)bis(ethylamine) (1.14 g) is added at room temperature
- 6workup.WAITfollowed by an overnight
- 7workup.STIRRINGstirring
- 8أخرىThe particles are then dialyzed
- 9workup.ADDITIONNext, they are dispersed in methanol (70 ml), to which 1 g of the chemical compound of Synthetic example 1
- 10workup.ADDITIONis added
- 11workup.WAITfollowed by a 6 hour
- 12workup.STIRRINGstirring at room temperature
- 13درجة الحرارةthis mixture is cooled in an ice bath
- 14workup.ADDITION2.8 g of sodium cyanotrihydroborate is added
- 15workup.WAITfollowed by an overnight
- 16workup.STIRRINGstirring at room temperature
- 17أخرىThe obtained particles are dialyzed in water
الإجراء التجريبي
Sodium dodecylsulfate (20 mg), N-isopropylacrylamide (2.7 g), acrylic acid (172 mg), and methylenebisacrylamide (121 mg) are dissolved in 200 ml of water, and, after a 30 minute stirring at 70° C. in a nitrogen atmosphere, a polymerization initiator (potassium persulfate 9.2 mg) is added, followed by 4 hours of stirring. The obtained particles (precursor of Example 1-2) are purified in water by means of dialysis, and then lyophilized. These particles are then dispersed in tetrahydrofuran (30 ml)/dimethylformamide (10 ml), and a tetrahydrofuran (10 ml)/dimethylformamide (50 ml) solution of dicyclohexylcarbodiimide (800 mg), hydroxybenzotriazole (500 mg), and 2,2′-(ethylenedioxy)bis(ethylamine) (1.14 g) is added at room temperature, followed by an overnight stirring. The particles are then dialyzed and lyophilized. Next, they are dispersed in methanol (70 ml), to which 1 g of the chemical compound of Synthetic example 1 is added, followed by a 6 hour stirring at room temperature; this mixture is cooled in an ice bath, 2.8 g of sodium cyanotrihydroborate is added, followed by an overnight stirring at room temperature. The obtained particles are dialyzed in water to obtain the target N-isopropylacrylamide/acrylic acid copolymer particles (620 mg) having phosphorylcholine groups directly on the particle surface.